[EN] PENICILLIN-BINDING PROTEIN INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉINE DE LIAISON À LA PÉNICILLINE
申请人:VENATORX PHARMACEUTICALS INC
公开号:WO2021108023A1
公开(公告)日:2021-06-03
Described herein are certain boron-containing compounds, compositions, preparations and their use as modulators of the transpeptidase function of bacterial penicillin-binding proteins and as antibacterial agents. In some embodiments, the compounds described herein inhibit penicillin-binding proteins. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections.
[EN] PENICILLIN-BINDING PROTEIN INHIBITORS<br/>[FR] INHIBITEURS DE PROTÉINES DE LIAISON À LA PÉNICILLINE
申请人:VENATORX PHARMACEUTICALS INC
公开号:WO2018218190A1
公开(公告)日:2018-11-29
Described herein are certain boron-containing compounds, compositions, preparations and their use as modulators of the transpeptidase function of bacterial penicillin-binding proteins and as antibacterial agents. In some embodiments, the compounds described herein inhibit penicillin-binding proteins. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections.
Beta-lactam Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel
申请人:BAYER AG
公开号:EP0003992A2
公开(公告)日:1979-09-19
β-Lactamvarbindungen der Formel
worin R Wasserstoff oder Alkoxy, B einen heterocyclischen Rest, A Äthylen, Trimethylen oder o-Phenylen, D eine Carbonylgruppe oder eine direkte Bindung und Z Wasserstoff oder einen Substituenten bedeuten, zeigen neben guter Verträglichkeit und Löslichkeit eine breite antibakterielle Wirkung sowie die Eigenschaft, das Wachstum und die Futterverwertung bei Tieren zu verbessam.
式中β-内酰胺化合物
其中 R 是氢或烷氧基,B 是杂环基,A 是乙烯、三亚甲基或邻亚苯基,D 是羰基或直接键,Z 是氢或取代基,这些化合物除了具有良好的相容性和溶解性外,还具有广泛的抗菌作用以及改善动物生长和饲料利用的特性。
Penicillin-binding protein inhibitors
申请人:VenatoRx Pharmaceuticals, Inc.
公开号:US11332485B2
公开(公告)日:2022-05-17
Described herein are certain boron-containing compounds, compositions, preparations and their use as modulators of the transpeptidase function of bacterial penicillin-binding proteins and as antibacterial agents. In some embodiments, the compounds described herein inhibit penicillin-binding proteins. In certain embodiments, the compounds described herein are useful in the treatment of bacterial infections.